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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

26635951 — Class I MDR by Rovipharm

MD Atlas
Rovipharm

EUDAMED last updated this device on Apr 13, 2026

26635951

3666663PDOS8V

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Rovipharm
UDI-DI code: 03666663000480
Reference / catalog number: 26635951

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Manufacturer information

Organization name: Rovipharm
SRN: FR-MF-000000673
Manufacturer status: Active

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26130101376033756PIBADQOn the market réducteur PF PP28 glass CE376033756PIBADQOn the market réducteur PF PP28 glass CE ENS376033756PIBADQOn the market Réglette Bronchodermine BL CE3666663REDOS53On the market 266368713666663PDOS8VOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03666663000480
Basic UDI-DI: 3666663PDOS8V
Reference / catalog number: 26635951
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 25
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0399MEASUREMENT DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification